| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:46104135-46104412 | Common:4; Rare:80; Clinvar (benign):1 | ||||
| chr18:46173895-46174086 | Common:1; Rare:49 | ||||
| chr18:46917370-46917669 | Common:3; Rare:125 | ||||
| chr18:47150442-47150554 | Common:3; Rare:42 | ||||
| chr18:49460599-49460814 | Common:2; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:49487159-49487328 | Common:2; Rare:64 | ||||
| chr18:49492131-49492591 | Common:5; Rare:169 | ||||
| chr18:49813489-49813637 | Rare:34 | ||||
| chr18:49813856-49814157 | Common:1; Rare:131 | ||||
| chr18:50281423-50281561 | Rare:53 | ||||
| chr18:50281750-50281899 | Rare:57 | ||||
| chr18:50374909-50375176 | Common:3; Rare:80 | ||||
| chr18:50878948-50879228 | Common:4; Rare:94 | ||||
| chr18:50967915-50968094 | Rare:63 | ||||
| chr18:51030041-51030227 | Rare:63 |